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1. Decadal-scale hotspot methane ebullition within lakes following abrupt permafrost thaw

   https://doi.org/10.1088/1748-9326/abc848  

   Walter Anthony, K. M.; Lindgren, P.; Hanke, P.; Engram, M.; Anthony, P.; Daanen, R. P.; Bondurant, A.; Liljedahl, A. K.; Lenz, J.; Grosse, G.; et al (February 2021, Environmental Research Letters)

   Abstract Thermokarst lakes accelerate deep permafrost thaw and the mobilization of previously frozen soil organic carbon. This leads to microbial decomposition and large releases of carbon dioxide (CO₂) and methane (CH₄) that enhance climate warming. However, the time scale of permafrost-carbon emissions following thaw is not well known but is important for understanding how abrupt permafrost thaw impacts climate feedback. We combined field measurements and radiocarbon dating of CH₄ebullition with (a) an assessment of lake area changes delineated from high-resolution (1–2.5 m) optical imagery and (b) geophysical measurements of thaw bulbs (taliks) to determine the spatiotemporal dynamics of hotspot-seep CH₄ebullition in interior Alaska thermokarst lakes. Hotspot seeps are characterized as point-sources of high ebullition that release¹⁴C-depleted CH₄from deep (up to tens of meters) within lake thaw bulbs year-round. Thermokarst lakes, initiated by a variety of factors, doubled in number and increased 37.5% in area from 1949 to 2009 as climate warmed. Approximately 80% of contemporary CH₄hotspot seeps were associated with this recent thermokarst activity, occurring where 60 years of abrupt thaw took place as a result of new and expanded lake areas. Hotspot occurrence diminished with distance from thermokarst lake margins. We attribute older¹⁴C ages of CH₄released from hotspot seeps in older, expanding thermokarst lakes (¹⁴C_CH420 079 ± 1227 years BP, mean ± standard error (s.e.m.) years) to deeper taliks (thaw bulbs) compared to younger¹⁴C_CH4in new lakes (¹⁴C_CH48526 ± 741 years BP) with shallower taliks. We find that smaller, non-hotspot ebullition seeps have younger¹⁴C ages (expanding lakes 7473 ± 1762 years; new lakes 4742 ± 803 years) and that their emissions span a larger historic range. These observations provide a first-order constraint on the magnitude and decadal-scale duration of CH₄-hotspot seep emissions following formation of thermokarst lakes as climate warms. 

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2. Assessing the Potential for Mobilization of Old Soil Carbon After Permafrost Thaw: A Synthesis of ¹⁴ C Measurements From the Northern Permafrost Region

   https://doi.org/10.1029/2020GB006672  

   Estop‐Aragonés, Cristian; Olefeldt, David; Abbott, Benjamin W.; Chanton, Jeffrey P.; Czimczik, Claudia I.; Dean, Joshua F.; Egan, Jocelyn E.; Gandois, Laure; Garnett, Mark H.; Hartley, Iain P.; et al (September 2020, Global Biogeochemical Cycles)

   Abstract The magnitude of future emissions of greenhouse gases from the northern permafrost region depends crucially on the mineralization of soil organic carbon (SOC) that has accumulated over millennia in these perennially frozen soils. Many recent studies have used radiocarbon (¹⁴C) to quantify the release of this “old” SOC as CO₂or CH₄to the atmosphere or as dissolved and particulate organic carbon (DOC and POC) to surface waters. We compiled ~1,900¹⁴C measurements from 51 sites in the northern permafrost region to assess the vulnerability of thawing SOC in tundra, forest, peatland, lake, and river ecosystems. We found that growing season soil¹⁴C‐CO₂emissions generally had a modern (post‐1950s) signature, but that well‐drained, oxic soils had increased CO₂emissions derived from older sources following recent thaw. The age of CO₂and CH₄emitted from lakes depended primarily on the age and quantity of SOC in sediments and on the mode of emission, and indicated substantial losses of previously frozen SOC from actively expanding thermokarst lakes. Increased fluvial export of aged DOC and POC occurred from sites where permafrost thaw caused soil thermal erosion. There was limited evidence supporting release of previously frozen SOC as CO₂, CH₄, and DOC from thawing peatlands with anoxic soils. This synthesis thus suggests widespread but not universal release of permafrost SOC following thaw. We show that different definitions of “old” sources among studies hamper the comparison of vulnerability of permafrost SOC across ecosystems and disturbances. We also highlight opportunities for future¹⁴C studies in the permafrost region. 

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3. Phosphonate cycling supports methane and ethylene supersaturation in the phosphate‐depleted western North Atlantic Ocean

   https://doi.org/10.1002/lno.11463  

   Sosa, Oscar A.; Burrell, Timothy J.; Wilson, Samuel T.; Foreman, Rhea K.; Karl, David M.; Repeta, Daniel J. (May 2020, Limnology and Oceanography)

   Abstract In oligotrophic ocean regions, dissolved organic phosphorus (DOP) plays a prominent role as a source of phosphorus (P) to microorganisms. An important bioavailable component of DOP is phosphonates, organophosphorus compounds with a carbon‐phosphorus (C‐P) bond, which are ubiquitous in high molecular weight dissolved organic matter (HMWDOM). In addition to being a source of P, the degradation of phosphonates by the bacterial C‐P lyase enzymatic pathway causes the release of trace hydrocarbon gases relevant to climate and atmospheric chemistry. In this study, we investigated the roles of phosphate and phosphonate cycling in the production of methane (CH₄) and ethylene (C₂H₄) in the western North Atlantic Ocean, a region that features a transition in phosphate concentrations from coastal to open ocean waters. We observed an inverse relationship between phosphate and the saturation state of CH₄and C₂H₄in the water column, and between phosphate and the relative abundance of the C‐P lyase marker genephnJ. In phosphate‐depleted waters, methylphosphonate and 2‐hydroxyethylphosphonate, the C‐P lyase substrates that yield CH₄and C₂H₄, respectively, were readily degraded in proportions consistent with their abundance and bioavailability in HMWDOM and with the concentrations of CH₄and C₂H₄in the water column. We conclude that phosphonate degradation through the C‐P lyase pathway is an important source and a common production pathway of CH₄and C₂H₄in the phosphate‐depleted surface waters of the western North Atlantic Ocean and that phosphate concentration can be an important control on the saturation state of these gases in the upper ocean. 

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4. High methane concentrations in tidal salt marsh soils: Where does the methane go?

   https://doi.org/10.1111/gcb.17050  

   Capooci, Margaret; Seyfferth, Angelia_L; Tobias, Craig; Wozniak, Andrew_S; Hedgpeth, Alexandra; Bowen, Malique; Biddle, Jennifer_F; McFarlane, Karis_J; Vargas, Rodrigo (November 2023, Global Change Biology)

   Abstract Tidal salt marshes produce and emit CH₄. Therefore, it is critical to understand the biogeochemical controls that regulate CH₄spatial and temporal dynamics in wetlands. The prevailing paradigm assumes that acetoclastic methanogenesis is the dominant pathway for CH₄production, and higher salinity concentrations inhibit CH₄production in salt marshes. Recent evidence shows that CH₄is produced within salt marshes via methylotrophic methanogenesis, a process not inhibited by sulfate reduction. To further explore this conundrum, we performed measurements of soil–atmosphere CH₄and CO₂fluxes coupled with depth profiles of soil CH₄and CO₂pore water gas concentrations, stable and radioisotopes, pore water chemistry, and microbial community composition to assess CH₄production and fate within a temperate tidal salt marsh. We found unexpectedly high CH₄concentrations up to 145,000 μmol mol⁻¹positively correlated with S²⁻(salinity range: 6.6–14.5 ppt). Despite large CH₄production within the soil, soil–atmosphere CH₄fluxes were low but with higher emissions and extreme variability during plant senescence (84.3 ± 684.4 nmol m⁻² s⁻¹). CH₄and CO₂within the soil pore water were produced from young carbon, with most Δ¹⁴C‐CH₄and Δ¹⁴C‐CO₂values at or above modern. We found evidence that CH₄within soils was produced by methylotrophic and hydrogenotrophic methanogenesis. Several pathways exist after CH₄is produced, including diffusion into the atmosphere, CH₄oxidation, and lateral export to adjacent tidal creeks; the latter being the most likely dominant flux. Our findings demonstrate that CH₄production and fluxes are biogeochemically heterogeneous, with multiple processes and pathways that can co‐occur and vary in importance over the year. This study highlights the potential for high CH₄production, the need to understand the underlying biogeochemical controls, and the challenges of evaluating CH₄budgets and blue carbon in salt marshes. 

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5. Methane production controls in a young thermokarst lake formed by abrupt permafrost thaw

   https://doi.org/10.1111/gcb.16151  

   Pellerin, André; Lotem, Noam; Walter Anthony, Katey; Eliani Russak, Efrat; Hasson, Nicholas; Røy, Hans; Chanton, Jeffrey P.; Sivan, Orit (March 2022, Global Change Biology)

   Abstract Methane (CH₄) release to the atmosphere from thawing permafrost contributes significantly to global CH₄emissions. However, constraining the effects of thaw that control the production and emission of CH₄is needed to anticipate future Arctic emissions. Here are presented robust rate measurements of CH₄production and cycling in a region of rapidly degrading permafrost. Big Trail Lake, located in central Alaska, is a young, actively expanding thermokarst lake. The lake was investigated by taking two 1 m cores of sediment from different regions. Two independent methods of measuring microbial CH₄ production, long term (CH₄accumulation) and short term (¹⁴C tracer), produced similar average rates of 11 ± 3.5 and 9 ± 3.6 nmol cm⁻³ d⁻¹, respectively. The rates had small variations between the different lithological units, indicating homogeneous CH₄production despite heterogeneous lithology in the surface ~1 m of sediment. To estimate the total CH₄production, the CH₄production rates were multiplied through the 10–15 m deep talik (thaw bulb). This estimate suggests that CH₄ production is higher than emission by a maximum factor of ~2, which is less than previous estimates. Stable and radioactive carbon isotope measurements showed that 50% of dissolved CH₄in the first meter was produced further below. Interestingly, labeled¹⁴C incubations with 2‐¹⁴C acetate and¹⁴C CO₂indicate that variations in the pathway used by microbes to produce CH₄depends on the age and type of organic matter in the sediment, but did not appear to influence the rates at which CH₄ was produced. This study demonstrates that at least half of the CH₄produced by microbial breakdown of organic matter in actively expanding thermokarst is emitted to the atmosphere, and that the majority of this CH₄is produced in the deep sediment. 

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